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1Treatment of acute periprosthetic infections with prosthesis retention: Review of current concepts显示文摘Periprosthetic joint infection(PJI) is a devastating complication after total joint arthroplasty, occurring in approximately 1%-2% of all cases. With growing populations and increasing age, PJI will have a growing effect on health care costs. Many risk factors have been identified that increase the risk of developing PJI, including obesity, immune system deficiencies, malignancy, previous surgery of the same joint and longer operating time. Acute PJI occurs either postoperatively(4 wk to 3 mo after initial arthroplasty, depending on the classification system), or via hematogenous spreading after a period in which the prosthesis had functioned properly. Diagnosis and the choice of treatment are the cornerstones to success. Although different definitions for PJI have been used in the past, most are more or less similar and include the presence of a sinus tract, blood infection values, synovial white blood cell count, signs of infection on histopathological analysis and one ormore positive culture results. Debridement, antibiotics and implant retention(DAIR) is the primary treatment for acute PJI, and should be performed as soon as possible after the development of symptoms. Success rates differ, but most studies report success rates of around 60%-80%. Whether single or multiple debridement procedures are more successful remains unclear. The use of local antibiotics in addition to the administration of systemic antibiotic agents is also subject to debate, and its pro's and con's should be carefully considered. Systemic treatment, based on culture results, is of importance for all PJI treatments. Additionally, rifampin should be given in Staphylococcal PJIs, unless all foreign material is removed. The most important factors contributing to treatment failure are longer duration of symptoms, a longer time after initial arthroplasty, the need for more debridement procedures, the retention of exchangeable components, and PJI caused by Staphylococcus(aureus or coagulase negative). If DAIR treatment is unsuccessful, the following treatment option should be based on the patient health status and his or her expectations. For the best functional outcome, one- or two-stage revision should be performed after DAIR failure. In conclusion, DAIR is the obvious choice for treatment of acute PJI, with good success rates in selected patients.Jesse WP Kuiper Robin Tjeenk Willink Dirk Jan F Moojen Michel PJ van den Bekerom Sascha Colen 2014World Journal of Orthopedics2014,5,5:12
2Radiotherapy plusconcomitant and adjuvant temozolomide for glioblastoma显示文摘Stupp R Mason WP van den Bent MJ 2005NEngl J Med2005,352,10:1
3Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma显示文摘STUPP R MASON WP VAN DEN BENT MJ 2005N Engl J Med2005,352,10:1
4Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma 显示文摘Stupp R Mason WP van den Bent M J 2005N Engl J Med2005,352,:1
52010 Update of the international ASAS recommendations for the use of anti-TNF agents in patients with axial spondyloarthritis显示文摘Van der Heijde D Sieper J Maksymowyeh WP 2011Ann Rheum Dis2011,70,6:1
6Cerebral microdialysis as a monitoring method in subarachnoid hemorrhage patients,and correlation with clinical events:a systematic review显示文摘 van Tulder MW Vandertop WP 2003J Neurol2003,250,:1
7Radiotherapy plus concomitant and adjuvant temozolomide for gliohlastoma显示文摘Stupp R Mason WP van den Bent MJ 2005N Engl J Med2005,352,10:1
8Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma显示文摘Stupp R Mason WP van den Bent MJ 2005N Engl J Med2005,352,10:1
9Treatment of ruptured intracranial aneurysms: implication of the ISAT on clipping versus coiling 显示文摘Van den Berg R Rinkel GJ Vandertop WP 2003Eur J Radial2003,46,3:1
10Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma 显示文摘Stupp R Mason WP Van den Bent M J 2005NEngl J Med2005,352,10:1
11Impact of cardiac complications on outcome after aneurysmal subarachnoid hemorrhage:ameta-analysis显示文摘Van der Bill IA Hasan D Vandertop WP 2009Neurology2009,72,7:1
12Cell-rather than antibody-mediated immunity leads to the development of profound thrombocytopenia during experimental Plasmodium berghei malaria显示文摘Van der Heyde HC Burns JM Weidanz WP 2005J Immunol2005,175,11:1
13The fetal variant of the circle of Willis and its influence on the cerebral collateral circulation 显示文摘Van Raamt AF Mali WP Van Laar PJ 2006Cerebrovasc Dis2006,22,4:1
1414-3-3η is a novel mediator associated with the pathogenesis of rheumatoid arthritis and joint damage显示文摘Maksymowych WP van der Heijde D Allaart CF 2014Arth Res Thera2014,16,2:1
15Surgery for large vestibular schwannoma:residual tumor and outcome显示文摘Godefroy WP van der Mey AG de Bruine FT 2009Otol Neurotol2009,30,5:1
16Universal mandatory health insurance in the Netherlands:a model for the United States显示文摘Van de Ven WP Schut FT 0,,:1
17Radiotherapyplus concomitant and adjuvant temozolomide for glioblas-toma 显示文摘Stupp R Mason WP van den Bent MJ 2005N Engl J Med2005,352,:1
18Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma显示文摘Stupp R Mason WP van den Bent MJ 2005N Engl J Med2005,352,10:1
19Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma 显示文摘Stupp R Mason WP van den Bent M J 2005N Engl J Med2005,352,:1
20Impact of goal - oriented and model - based clinical pharmacokinetic dosing of aminoglyucosides on clinical outcome: a cost -effectiveness analysis 显示文摘Van Lent Evens NA Mathot RA Gens WP 1999Ther Drug Monit1999,21,1:1
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